Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Evgeni Vlaev"'
Autor:
M. E. Ketelaar, K. Van De Kant, F. N. Dijk, E. M. M. Klaassen, N. Grotenboer, M. C. Nawijn, E. Dompeling, G. H. Koppelman, Clare Murray, Philip Foden, Lesley Lowe, Hannah Durrington, Adnan Custovic, Angela Simpson, Andrew J. Simpson, Dominick E. Shaw, Ana R. Sousa, Louise J. Fleming, Graham Roberts, Ioannis Pandis, Aruna T. Bansal, Julie Corfield, Scott Wagers, Ratko Djukanovic, Kian Fan Chung, Peter J. Sterk, Jorgen Vestbo, Stephen J. Fowler, S. J. Tebbutt, A. Singh, C. P. Shannon, Y. W. Kim, C. X. Yang, G. M. Gauvreau, J. M. Fitzgerald, L. P. Boulet, P. M. O’Byrne, N. Begley, A. Loudon, D. W. Ray, Selene Baos, Lucía Cremades, David Calzada, Carlos Lahoz, Blanca Cárdaba, Kewal Asosingh, Chris Lauruschkat, Kimberly Queisser, Nicholas Wanner, Kelly Weiss, Weiling Xu, Serpil Erzurum, Milena Sokolowska, Li-Yuan Chen, Yueqin Liu, Asuncion Martinez-Anton, Carolea Logun, Sara Alsaaty, Rosemarie Cuento, Rongman Cai, Junfeng Sun, Oswald Quehenberger, Aaron Armando, Edward Dennis, Stewart Levine, James Shelhamer, Kilyong Choi, Snezhina Lazova, Penka Perenovska, Dimitrinka Miteva, Stamatios Priftis, Guergana Petrova, Vassil Yablanski, Evgeni Vlaev, Hristina Rafailova, Takashi Kumae, L. J. Holmes, J. Yorke, D. M. Ryan, Sasawan Chinratanapisit, Khlongtip Matchimmadamrong, Jitladda Deerojanawong, Wissaroot Karoonboonyanan, Paskorn Sritipsukho, Vania Youroukova, Denitsa Dimitrova, Yanina Slavova, Spaska Lesichkova, Iren Tzocheva, Snezhana Parina, Svetla Angelova, Neli Korsun, Mihai Craiu, Iustina Violeta Stan, Matea Deliu, Tolga Yavuz, Matthew Sperrin, Umit M. Sahiner, Danielle Belgrave, Cansin Sackesen Sackesen, Ömer Kalayci, Petar Velikov, Tsvetelina Velikova, Ekaterina Ivanova-Todorova, Kalina Tumangelova-Yuzeir, Dobroslav Kyurkchiev, Spyridon Megremis, Bede Constantinides, Alexandros Georgios Sotiropoulos, Paraskevi Xepapadaki, David Robertson, Nikolaos Papadopoulos, Maxim Wilkinson, Craig Portsmouth, David Ray, Royston Goodacre, Anna Valerieva, Irina Bobolea, Daiana Guillén Vera, Gabriel Gonzalez-Salazar, Carlos Melero Moreno, Consuelo Fernandez Rodriguez, Natividad De Las Cuevas Moreno, R. Wang, I. Satia, R. Niven, J. A. Smith, T. Southworth, J. Plumb, V. Gupta, J. Pearson, I. Ramis, M. D. Lehner, M. Miralpeix, D. Singh, Imran Satia, Mark Woodhead, Paul O’Byrne, Jaclyn Ann Smith, Cecilia Forss, Peter Cook, Sheila Brown, Freya Svedberg, Katherine Stephenson, Margherita Bertuzzi, Elaine Bignell, Malin Enerbäck, Danen Cunoosamy, Andrew Macdonald, Caini Liu, Liang Zhu, Kiochi Fukuda, Cunjin Zhang, Suidong Ouyang, Xing Chen, Luke Qin, Suguna Rachakonda, Mark Aronica, Jun Qin, Xiaoxia Li, Marie-Chantal Larose, Anne-Sophie Archambault, Véronique Provost, Jamila Chakir, Michel Laviolette, Nicolas Flamand, Nicola Logan, Dominik Ruckerl, Judith E. Allen, Tara E. Sutherland, E. Hamelmann, C. Vogelberg, S. Goldstein, G. E. Azzi, M. Engel, R. Sigmund, S. J. Szefler, Raquel Mesquita, Luis Coentrão, Rui Veiga, José-Artur Paiva, Roberto Roncon-Albuquerque, Wendy Vargas Porras, Ana González Moreno, Jesus Macías Iglesias, Gustavo Córdova Ramos, Yesenia Peña Acevedo, Miguel Angel Tejedor Alonso, Maria Del Mar Moro Moro, Irena Krcmova, Jakub Novosad, Nicola Alexander Hanania, Marc Massanari, Heike Hecker, Eric Kassel, Craig Laforce, Kathy Rickard, Sanne Snelder, Gert-Jan Braunstahl, T. L. Jones, D. Neville, E. R. Heiden, E. Lanning, T. Brown, H. Rupani, K. S. Babu, A. J. Chauhan, M. Y. Eldegeir, A. A. Chapman, M. Ferwana, M. Caldron
Publikováno v:
Clinical and Translational Allergy, Vol 7, Iss S2, Pp 1-17 (2017)
Externí odkaz:
https://doaj.org/article/8aa220adbd1b41528cac7a760f22478f
Autor:
Stamatios Priftis, Snezhina Lazova, Evgeni Vlaev, Emilia Naseva, Vasil Yablanski, Penka Perenovska, Guergana Petrova
Publikováno v:
Annals of Pulmonology. 3
Scoliosis is the most common abnormality of the spine with direct effects on the thoracic cage, leading to potentially severe and irreversible changes in lung function. Scoliosis has generally been associated with the development of restrictive lung
Publikováno v:
Journal of Clinical and Experimental Investigations, Vol 7, Iss 3, Pp 216-221 (2016)
Volume: 7, Issue: 3 216-221
Journal of Clinical and Experimental Investigations
Volume: 7, Issue: 3 216-221
Journal of Clinical and Experimental Investigations
Objectives: The association studies are the predominant type of studies on genetics of the common diseases. The pre-sent case-control study aims to investigate the association between the promoter polymorphism TPH1 (rs10488682 T/A) and the predisposi
Autor:
Alexandre Loukanov, Evgeni Vlaev, Luben Stokov, Vasil Yablanski, Svetla Nikolova, Alexey Savov, Ivo Kremensky
Publikováno v:
SPINE. 41:785-791
A case-control study was performed on 105 patients with idiopathic scoliosis (IS) and 210 unrelated gender-matched controls from Bulgarian population.Investigation of the association between common genetic polymorphisms of IL-6 and MMP3 genes and the
Autor:
Khlongtip Matchimmadamrong, J. Yorke, M. C. Nawijn, David Robertson, Serpil C. Erzurum, Evgeni Vlaev, Matthew Sperrin, Cecilia Forss, Jun Qin, A. A. Chapman, E. M. M. Klaassen, K. S. Babu, Tsvetelina Velikova, Consuelo Fernandez Rodriguez, Natividad De Las Cuevas Moreno, Rui Veiga, Nicola Logan, Clare S. Murray, Dominick E. Shaw, Vandana Gupta, Peter C. Cook, Li-Yuan Chen, Junfeng Sun, Louise Fleming, Sanne M. Snelder, Irina Bobolea, Dave Singh, N. Begley, James Shelhamer, Xing Chen, Kimberly Queisser, Gabriel Gonzalez-Salazar, Dan Neville, Freya Svedberg, Andrew Simpson, Jamila Chakir, C. P. Shannon, L. J. Holmes, Mark Woodhead, Philip Foden, Maria Del Mar Moro Moro, Yueqin Liu, Judith E. Allen, Gail M. Gauvreau, Paskorn Sritipsukho, Gustavo Córdova Ramos, Caini Liu, Miguel Angel Tejedor Alonso, Liang Zhu, Peter J. Sterk, Xiaoxia Li, David W. Ray, Stan Szefler, E. Dompeling, Blanca Cárdaba, Edward Dennis, Daiana Guillén Vera, Rosemarie Cuento, Oswald Quehenberger, Ana González Moreno, Kathy Rickard, Ellie Lanning, Kalina Tumangelova-Yuzeir, Eckard Hamelmann, Bede Constantinides, Tom C. Brown, M. Caldron, G. E. Azzi, Marie-Chantal Larose, Carlos Lahoz, Luis Coentrão, Andrew Macdonald, Penka Perenovska, Michael Engel, F. N. Dijk, Yesenia Peña Acevedo, S. J. Tebbutt, M. E. Ketelaar, I. Satia, Weiling Xu, Nicolas Flamand, Isabel Ramis, José-Artur Paiva, Maxim Wilkinson, Martin D. Lehner, J. M. Fitzgerald, Eric Kassel, Nicholas Wanner, Takashi Kumae, Y. W. Kim, N. Grotenboer, S. Goldstein, Montserrat Miralpeix, Kian Fan Chung, Omer Kalayci, Véronique Provost, Umit Murat Sahiner, Anne-Sophie Archambault, M. Ferwana, Milena Sokolowska, M. Y. Eldegeir, Svetla Angelova, Sasawan Chinratanapisit, David Calzada, Kilyong Choi, Nikolaos G. Papadopoulos, Matea Deliu, Spaska Lesichkova, Roberto Roncon-Albuquerque, Ana R. Sousa, Scott Wagers, Tolga S Yavuz, Vassil Yablanski, Margherita Bertuzzi, D. M. Ryan, Carlos Melero Moreno, Carolea Logun, Christian Vogelberg, Elaine Bignell, Petar Velikov, Ratko Djukanovic, Ralf Sigmund, Anna Valerieva, Spyridon Megremis, Snezhina Lazova, R. Niven, A. Singh, Danen Cunoosamy, Paraskevi Xepapadaki, Craig Laforce, Wendy Vargas Porras, Aruna T. Bansal, Adnan Custovic, Michel Laviolette, Chris Lauruschkat, Jakub Novosad, Katherine Stephenson, Jesus Macías Iglesias, Paul M. O'Byrne, R. Wang, Yanina Slavova, K.D.G. van de Kant, Cunjin Zhang, Ekaterina Ivanova-Todorova, Wissaroot Karoonboonyanan, Iren Tzocheva, Tara E. Sutherland, Jørgen Vestbo, Selene Baos, Mihai Craiu, Andrew S. I. Loudon, Guergana Petrova, Aaron Armando, Danielle Belgrave, Dimitrinka Miteva, Suguna Rachakonda, Lucía Cremades, Craig Portsmouth, Royston Goodacre, Marc Massanari, Sheila Brown, C. X. Yang, Irena Krčmová, Louis P. Boulet, Suidong Ouyang, Snezhana Parina, Thomas Southworth, Vania Youroukova, Sara Alsaaty, Anoop Chauhan, P. M. O’Byrne, Emily Heiden, Mark A. Aronica, Hristina Rafailova, J. Pearson, Kelly Weiss, J. A. Smith, Imran Satia, Angela Simpson, Dominik Rückerl, Dobroslav Kyurkchiev, Jitladda Deerojanawong, Asuncion Martinez-Anton, Kiochi Fukuda, Graham Roberts, Neli Korsun, Jaclyn A. Smith, Kewal Asosingh, Lesley Lowe, Gerard H. Koppelman, Nicola A. Hanania, Stewart Levine, Raquel Mesquita, Denitsa Dimitrova, Stamatios Priftis, Heike Hecker, Hannah J. Durrington, Ioannis Pandis, Julie Corfield, Hitasha Rupani, D. W. Ray, Iustina Violeta Stan, Thomas Jones, Gert-Jan Braunstahl, Alexandros Georgios Sotiropoulos, Rongman Cai, Luke Qin, Stephen J. Fowler, Malin Enerbäck, Jonathan Plumb, Cansin Sackesen
Publikováno v:
Clinical and Translational Allergy, Vol 7, Iss S2, Pp 1-17 (2017)
Clinical and Translational Allergy
Clinical and Translational Allergy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::40cc18db6eab3156f3652b00109b0190
Publikováno v:
Journal of Biomarkers
The concept of disease-modifier genes as an element of genetic heterogeneity has been widely accepted and reported. The aim of the current study is to investigate the association between the promoter polymorphism TPH1 (rs10488682) and progression of
Publikováno v:
Open Access Macedonian Journal of Medical Sciences; Vol. 3 No. 2 (2015): Jun 15 (OAMJMS); 278-282
Open Access Macedonian Journal of Medical Sciences
Open Access Macedonian Journal of Medical Sciences, Vol 3, Iss 2, Pp 278-282 (2015)
Open Access Macedonian Journal of Medical Sciences; Vol 3, No 2 (2015): Jun 15 (OAMJMS); 278-282
Open Access Macedonian Journal of Medical Sciences
Open Access Macedonian Journal of Medical Sciences, Vol 3, Iss 2, Pp 278-282 (2015)
Open Access Macedonian Journal of Medical Sciences; Vol 3, No 2 (2015): Jun 15 (OAMJMS); 278-282
BACKGROUND: The current consensus on idiopathic scoliosis maintains that it has a multifactorial etiology with genetic predisposing factors.AIM: Estrogen receptor alpha gene has been considered as candidate gene of idiopathic scoliosis.MATERIAL AND M
Publikováno v:
Genetics Research International, Vol 2015 (2015)
Genetics Research International
Genetics Research International
Idiopathic scoliosis (IS) is a complex genetic disorder of the musculoskeletal system, characterized by three-dimensional rotation of the spine with unknown etiology. For the aims of the current study we selected 3 single nucleotide polymorphisms wit